Appetite Responses to Breakfast Bar Product
1 other identifier
interventional
120
1 country
1
Brief Summary
The purpose of this clinical trial is to investigate appetite responses to 2 cereal products in healthy adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 21, 2024
CompletedFirst Posted
Study publicly available on registry
August 23, 2024
CompletedStudy Start
First participant enrolled
October 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 24, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
October 24, 2024
CompletedJanuary 13, 2025
January 1, 2025
4 days
August 21, 2024
January 10, 2025
Conditions
Outcome Measures
Primary Outcomes (6)
Visual Analogue Scale for Hunger 0-240 minutes
Visual Analogue Scale for "how hungry are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more hunger. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
240 minutes
Visual Analogue Scale for Fullness 0-240 minutes
Visual Analogue Scale for "how full are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more fullness. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
240 minutes
Visual Analogue Scale for Satiation 0-240 minutes
Visual Analogue Scale for "how satiated are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satiation. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
240 minutes
Visual Analogue Scale for Desire to Eat 0-240 minutes
Visual Analogue Scale for "how strong is your desire to eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more desire to eat. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
240 minutes
Visual Analogue Scale for Prospective Consumption 0-240 minutes
Visual Analogue Scale for "how much do you think you can eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more prospective consumption. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
240 minutes
Visual Analogue Scale for Satisfaction 0-240 minutes
Visual Analogue Scale for "how satisfied are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satisfaction. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
240 minutes
Study Arms (2)
Breakfast Bar
EXPERIMENTALPackaged breakfast bar available in retail stores
Control
NO INTERVENTIONNo intervention (i.e., no food provided)
Interventions
Eligibility Criteria
You may qualify if:
- Healthy adults 18-70 years
- Habitual snack bar consumers (at least several times per month)
- Body mass index 18.5-29.9 kg/m2 (based on self-reported weight and height)
- Understand and willing to follow the study procedures
- Willing to maintain habitual diet, physical activity pattern, and body weight throughout the trial
- Willing to abstain from strenuous exercise, consuming alcoholic drinks 24 hours before the test day
- Willing to provide informed consent to participate in the study
You may not qualify if:
- Pregnant or lactating women, or women who are planning to become pregnant during the study
- Known food allergies, sensitivities, or intolerance to any food or food ingredients
- Participating in another clinical trial for food, investigational drug, nutritional supplement, or lifestyle modification
- Taking medications that affect appetite, metabolism or blood pressure
- Presence of acute diseases or infection
- Presence or history of chronic diseases
- Diagnosed with an eating disorder
- Restraint eaters as determined by a score \>4 from the Dutch Eating Behavior Questionnaire
- Lost or gained 5 or more pounds in the past 3-months
- On a weight loss diet or undergoing intermittent fasting
- COVID-19 infection within the past 3 months
- Subjects who do not eat bar products
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- General Millslead
Study Sites (1)
Remote
Minneapolis, Minnesota, 55430, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 21, 2024
First Posted
August 23, 2024
Study Start
October 20, 2024
Primary Completion
October 24, 2024
Study Completion
October 24, 2024
Last Updated
January 13, 2025
Record last verified: 2025-01
Data Sharing
- IPD Sharing
- Will not share